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Long-term outcomes of two rescue therapies in lamivudine-refractory patients with chronic hepatitis B: combined lamivudine and adefovir, and 1-mg entecavir

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dc.contributor.authorZe, E.-
dc.contributor.authorBaek, E.K.-
dc.contributor.authorLee, J.J.-
dc.contributor.authorChung, H.W.-
dc.contributor.authorAhn, D.G.-
dc.contributor.authorCho, H.J.-
dc.contributor.authorKwon, J.C.-
dc.contributor.authorKim, H.J.-
dc.contributor.authorLee, H.-
dc.date.available2019-03-09T00:41:15Z-
dc.date.issued2014-09-
dc.identifier.issn2287-285X-
dc.identifier.issn2287-285X-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/13896-
dc.description.abstractBACKGROUND/AIMS: Adefovir (ADV) and lamivudine (LAM) combination therapy (ADV+LAM) has been a useful option for patients with LAM-resistant (LAM-r) chronic hepatitis B (CHB). However, the long-term outcomes of LAM+ADV and 1-mg entecavir (ETV) rescue therapies have still been limited. The aim of this study was to determine the long-term outcomes of these two rescue therapies.METHODS: Sixty patients with LAM-r CHB underwent rescue therapy with LAM+ADV (n=36) or 1-mg ETV (n=24). We determined the duration of rescue therapy, timing and type of mutation, undetectable serum hepatitis B virus (HBV) DNA by PCR (lower limitation of detection, < 140 copies/mL), biochemical response (alanine aminotransferase < 40 IU/mL), and the incidence of hepatitis B virus e antigen (HBeAg) seroconversion and virologic breakthrough.RESULTS: Baseline characteristics did not differ between the two therapy groups. The duration of rescue therapy was 56 months (range, 14-100 months) in the ADV+LAM group and 42 months (range, 12-73 months) in the ETV group (P=0.036). The cumulative rates of HBV DNA undetectability and HBeAg seroconversion up to 6 years were 88.6% and 43.0%, respectively, in the ADV+LAM group, and 45.8% and 31.8% in the ETV group. The rate of virologic breakthrough and resistance was 14.4% in the ADV+LAM group and 71.9% in the ETV group (P=0.001).CONCLUSIONS: Combination of LAM and ADV therapy for up to 6 years achieved modest rates of virological suppression and resistance. ETV is not an optimal therapy because the risk of viral breakthrough to ETV increases over time.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisher대한간학회-
dc.titleLong-term outcomes of two rescue therapies in lamivudine-refractory patients with chronic hepatitis B: combined lamivudine and adefovir, and 1-mg entecavir-
dc.title.alternativeLong-term outcomes of two rescue therapies in lamivudine- refractory patients with chronic hepatitis B: combined lamivudine and adefovir, and 1-mg entecavir-
dc.typeArticle-
dc.identifier.doi10.3350/cmh.2014.20.3.267-
dc.identifier.bibliographicCitationClinical and molecular hepatology, v.20, no.3, pp 267 - 273-
dc.identifier.kciidART001920532-
dc.description.isOpenAccessN-
dc.identifier.scopusid2-s2.0-84932104604-
dc.citation.endPage273-
dc.citation.number3-
dc.citation.startPage267-
dc.citation.titleClinical and molecular hepatology-
dc.citation.volume20-
dc.type.docTypeArticle-
dc.publisher.location대한민국-
dc.subject.keywordAuthorAdefovir-
dc.subject.keywordAuthorChronic hepatitis B-
dc.subject.keywordAuthorEntecavir-
dc.subject.keywordAuthorLamivudine-
dc.subject.keywordAuthorResistance-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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